A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727459



Internal ID17871981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39844406..39855436hg38UCSC Ensembl
Innerchr9:41989424..42000454hg19UCSC Ensembl
Innerchr9:41979424..41990454hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3811031
hg1911031
hg1811031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973238
Supporting Variants
SamplesHGDP01284
Known GenesKGFLP2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2727459
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer